Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:42755778-42756068 | Common:1; Rare:51 | ||||
chr21:42758782-42759058 | Common:2; Rare:68 | ||||
chr21:42768994-42769325 | Common:7; Rare:121 | ||||
chr21:43326076-43326378 | Common:2; Rare:67 | ||||
chr21:43361842-43361952 | Rare:26 | ||||
chr21:43719884-43720172 | Rare:60 | ||||
chr21:44316235-44316524 | Common:3; Rare:104 | ||||
chr21:46116649-46116814 | Rare:73; Clinvar:6; Clinvar (benign):5 | ||||
chr21:46254447-46254616 | Common:1; Rare:50 | ||||
chr21:46429818-46430032 | Common:1; Rare:69 | ||||
chr22:17266542-17266711 | Rare:30 | ||||
chr22:17893939-17894108 | Common:1; Rare:35 | ||||
chr22:19171606-19171724 | Rare:37 | ||||
chr22:19401630-19401666 | Rare:4 | ||||
chr22:20956104-20956396 | Rare:56 |